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Miglustat hydrochloride

Base Information
  • Chemical Name:Miglustat hydrochloride
  • CAS No.:210110-90-0
  • Molecular Formula:C10H22ClNO4
  • Molecular Weight:255.742
  • Hs Code.:2933399990
  • European Community (EC) Number:874-729-5
  • ChEMBL ID:CHEMBL1329690
  • Mol file:210110-90-0.mol
Miglustat hydrochloride

Synonyms:210110-90-0;Miglustat hydrochloride;Miglustat (hydrochloride);N-Butyldeoxynojirimycin, Hydrochloride;N-Butyldeoxynojirimycin hydrochloride;SMR000058560;(2R,3R,4R,5S)-1-butyl-2-(hydroxymethyl)piperidine-3,4,5-triol hydrochloride;MLS000069516;Miglustat HCl;Opera_ID_475;N-Butyldeoxynojirimycin HCl;CHEMBL1329690;SCHEMBL11898780;NB-DNJ hydrochloride;OGT918 hydrochloride;N-Butyldeoxynojirimycin middot HCl;HY-17020A;MFCD00269940;AKOS024457437;N-Butyldeoxynojirimycin;AC-33704;AS-79087;N-(n-Butyl)deoxynojirimycin hydrochloride;N-Butyl-DNJ,HCl;Miglustat(hydrochloride);E73460;A912326;EN300-19750339;N-(N-BUTYL)DEOXYNOJIRIMYCIN, HYDROCHLORIDE;W-201839;(2R,3R,4R,5S)-1-Butyl-2-(hydroxymethyl)-,3,4,5-Piperidinetriol Hydrochloride;(2R,3R,4R,5S)-1-Butyl-2-(hydroxymethyl)-3,4,5-piperidinetriol hydrochloride;3,4,5-Piperidinetriol, 1-butyl-2-(hydroxymethyl)-, hydrochloride (1:1), (2R,3R,4R,5S)-

Suppliers and Price of Miglustat hydrochloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • N-Butyldeoxynojirimycin, Hydrochloride
  • 10mg
  • $ 418.00
  • Usbiological
  • N-Butyldeoxynojirimycin HCl
  • 5mg
  • $ 389.00
  • TRC
  • N-Butyldeoxynojirimycin, Hydrochloride
  • 50mg
  • $ 570.00
  • Tocris
  • Miglustathydrochloride
  • 10
  • $ 227.00
  • Medical Isotopes, Inc.
  • N-ButyldeoxynojirimycinHCl
  • 50 mg
  • $ 1960.00
  • DC Chemicals
  • Miglustat(hydrochloride) >98%
  • 1 g
  • $ 3000.00
  • DC Chemicals
  • Miglustat(hydrochloride) >98%
  • 250 mg
  • $ 1500.00
  • Crysdot
  • Miglustathydrochloride 98+%
  • 5mg
  • $ 59.00
  • Crysdot
  • Miglustathydrochloride 98+%
  • 10mg
  • $ 104.00
  • Cayman Chemical
  • N-Butyldeoxynojirimycin (hydrochloride) ≥98%
  • 1mg
  • $ 32.00
Total 19 raw suppliers
Chemical Property of Miglustat hydrochloride
Chemical Property:
  • Vapor Pressure:7.37E-09mmHg at 25°C 
  • Melting Point:169-172°C 
  • Boiling Point:421.2°C at 760 mmHg 
  • Flash Point:208.5°C 
  • PSA:84.16000 
  • LogP:-0.71440 
  • Storage Temp.:Desiccate at -20°C 
  • Solubility.:Soluble in DMSO (up to 20 mg/ml) or in Water (up to 20 mg/ml) 
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:255.1237359
  • Heavy Atom Count:16
  • Complexity:190
Purity/Quality:

99%, *data from raw suppliers

N-Butyldeoxynojirimycin, Hydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCN1CC(C(C(C1CO)O)O)O.Cl
  • Isomeric SMILES:CCCCN1C[C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O.Cl
  • Description Miglustat HCl (210110-90-0) is an orally active ceramide-specific glycosyltransferase and α-glucosidase I and II inhibitor.1 Rescues trafficking-deficient F508del-CFTR in human airway epithelial cells via inhibition of ER α-glucosidases I and II.2 Pharmacological chaperone for glucocerebrosidase degradation.3 Clinically useful agent for Gaucher disease type 1.4 Stabilizes neurological disorders in Niemann-Pick disease type C.5
  • Uses An inhibitor of a-glucosidase 1 as well as being an inhibitor of HIV cytopathicity. N-Butyldeoxynojirimycin has recently been used to retard lipid storage in the central nervous system of an animal m odel of Tay-Sachs disease. 1-Deoxynojirimycin derivatives as selective inhibitors of glucosylceramide metabolism in man.
Technology Process of Miglustat hydrochloride

There total 1 articles about Miglustat hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene;
Downstream raw materials:

N-butyldeoxynojirimycin

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